Copy number loss in SFMBT1 is common among Finnish and Norwegian patients with iNPH

OBJECTIVE: To evaluate the role of the copy number loss in SFMBT1 in a Caucasian population. METHODS: Five hundred sixty-seven Finnish and 377 Norwegian patients with idiopathic normal pressure hydrocephalus (iNPH) were genotyped and compared with 508 Finnish elderly, neurologically healthy controls...

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Publicat a:Neurol Genet
Autors principals: Korhonen, Ville E., Helisalmi, Seppo, Jokinen, Aleksi, Jokinen, Ilari, Lehtola, Juha-Matti, Oinas, Minna, Lönnrot, Kimmo, Avellan, Cecilia, Kotkansalo, Anna, Frantzen, Janek, Rinne, Jaakko, Ronkainen, Antti, Kauppinen, Mikko, Junkkari, Antti, Hiltunen, Mikko, Soininen, Hilkka, Kurki, Mitja, Jääskeläinen, Juha E., Koivisto, Anne M., Sato, Hidenori, Kato, Takeo, Remes, Anne M., Eide, Per Kristian, Leinonen, Ville
Format: Artigo
Idioma:Inglês
Publicat: Wolters Kluwer 2018
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Article
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC6283454/
https://ncbi.nlm.nih.gov/pubmed/30584596
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1212/NXG.0000000000000291
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